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FDA 510(k) Applications Submitted by COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110268
01/28/2011
FORCETRIAD ELECTROSURGICAL GENERATOR
COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON
K072687
09/24/2007
VALLEYLAB MICROWAVE ABLATION GENERATOR
COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON
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